Trans-2-(3,5-difluorophenyl)vinyl boronic acid pinacol ester


Chemical Name: Trans-2-(3,5-difluorophenyl)vinyl boronic acid pinacol ester
CAS Number: 1073354-58-1
Product Number: AG007WHO(AGN-PC-0WAFEV)
Synonyms:
MDL No:
Molecular Formula: C14H17BF2O2
Molecular Weight: 266.0914

Identification/Properties


Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


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Chemical Structure



(E)-2-(3,5-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, commonly referred to as $name$, is a versatile compound utilized in various chemical synthesis processes. Its application in organic chemistry is particularly noteworthy, as it serves as a valuable building block in the creation of complex molecules.In chemical synthesis, (E)-2-(3,5-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane acts as a key component for the introduction of difluorostyryl groups into target molecules. This compound's unique structure enables precise control over the steric and electronic properties of the final products, making it a preferred choice for chemists aiming to design molecules with specific functional characteristics.Furthermore, (E)-2-(3,5-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane's reactivity and stability under various reaction conditions make it a reliable reagent in synthetic processes. Its compatibility with a wide range of reaction conditions expands its utility in the development of new materials, pharmaceuticals, and agrochemicals.Overall, the strategic incorporation of (E)-2-(3,5-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis empowers chemists to explore novel molecular structures and functionalities, driving innovation in the field of organic chemistry.